胞苷脱氨酶
脱氨基
阿波贝克
体细胞突变
活化诱导(胞苷)脱氨酶
生物
胞苷
DNA
遗传学
基因组
基因组不稳定性
分子生物学
生物化学
酶
基因
DNA损伤
抗体
B细胞
作者
Rachel A. DeWeerd,Abby M. Green
出处
期刊:Methods in molecular biology
日期:2022-01-01
卷期号:: 161-169
标识
DOI:10.1007/978-1-0716-2063-2_10
摘要
The human genome encodes eleven DNA cytidine deaminases in the AID/APOBEC family, which encompass endogenous roles ranging from genetic diversification of the immunoglobulin locus to virus restriction. All AID/APOBEC functions are enabled by their catalyzation of cytidine deamination resulting in mutations and DNA damage. When acting aberrantly, deaminases can cause off-target mutations in the cellular genome resulting in somatic mutations, DNA damage, and genome instability. An association between cytidine deaminase-induced mutations and human cancers has been recognized over the last decade, necessitating assays for investigation of intracellular deaminase activity. Here we present two assays for deamination activity which enable in vitro evaluation of in vivo events. We define both a qualitative assay to confirm deaminase activity within cells as well as a quantitative assay for granular evaluation and comparisons of deamination activity across different cell populations or experimental conditions. The two procedures are customizable assays which can easily be adapted to individual labs and experiments.
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